Process for improving the selectivity of an eo catalyst

ABSTRACT

The present invention relates to a process for improving the overall selectivity of an EO process for converting ethylene to ethylene oxide utilizing a highly selective EO silver catalyst containing a rhenium promoter wherein following normal operation a hard strip of the chloride on the surface of the catalyst is conducted in order to remove a portion of the chlorides on the surface of the catalyst. Following the hard strip, the catalyst is optionally re-optimized. Surprisingly, it has been found that the selectivity of the catalyst following the hard strip may be substantially higher than the selectivity prior to the hard strip.

This application claims the benefit of U.S. Provisional Application 61/420,844 filed Dec. 8, 2010, which is herein incorporated by reference.

FIELD OF THE INVENTION

The invention relates to a process for the operation of an ethylene epoxidation process which employs a silver-based highly selective epoxidation catalyst. The invention also relates to a process for the production of ethylene oxide, a 1,2-diol, a 1,2-diol ether, a 1,2-carbonate, or an alkanolamine.

BACKGROUND OF THE INVENTION

In olefin epoxidation an olefin is reacted with oxygen to form an olefin epoxide, using a catalyst comprising a silver component, usually with one or more further elements deposited therewith on a support. The olefin oxide may be reacted with water, an alcohol, carbon dioxide or an amine to form a 1,2-diol, a 1,2-diol ether, 1,2 carbonate or an alkanolamine. Thus, 1,2-diols, 1,2-diol ethers and alkanolamines may be produced in a multi-step process comprising olefin epoxidation and converting the formed olefin oxide with water, an alcohol or an amine.

The performance of the epoxidation process may be assessed on the basis of the selectivity, the catalyst's activity, and stability of operation. The selectivity is the molar fraction of the converted olefin yielding the desired olefin oxide. Modern silver-based epoxidation catalysts are highly selective towards olefin oxide production. When using the modern catalysts in the epoxidation of ethylene the selectivity towards ethylene oxide can reach values above 85 mole-%. An example of such highly selective catalysts is a catalyst comprising silver and a rhenium promoter, for example U.S. Pat. No. 4,761,394 and U.S. Pat. No. 4,766,105.

For decades much research has been devoted to improving the activity, the selectivity, and the lifetime of the catalysts, and to find process conditions which enable full exploitation of the catalyst performance. A reaction modifier, for example an organic halide, may be added to the feed in an epoxidation process for increasing the selectivity of a highly selective catalyst (see for example EP-A-352850, U.S. Pat. No. 4,761,394 and U.S. Pat. No. 4,766,105, which are herein incorporated by reference). The reaction modifier suppresses the undesirable oxidation of olefin or olefin oxide to carbon dioxide and water, relative to the desired formation of olefin oxide. EP-A-352850 teaches that there is an optimum in the selectivity as a function of the quantity of organic halide in the feed, at a constant oxygen conversion level and given set of reaction conditions.

Many process improvements are known that can improve selectivity. For example, it is well known that low CO₂ levels are useful in improving the selectivity of high selectivity catalysts. See, e.g., U.S. Pat. No. 7,235,677; U.S. Pat. No. 7,193,094; US Pub. Pat. App. 2007/0129557; WO 2004/078736; WO 2004/078737; and EP 2,155,708. These patents also disclose that water concentration in the reactor feed should be maintained at a level of at most 0.35 mole percent, preferably less than 0.2 mole percent. Other patents disclose control of the chloride moderator to maintain good activity. See, e.g., U.S. Pat. No. 7,657,331; EP 1,458,698; and U.S. Pub. Pat. App. 2009/0069583. Still further, there are many other patents dealing with EO process operation and means to improve the performance of the catalyst in the process. See, e.g., U.S. Pat. Nos. 7,485,597, 7,102,022, 6,717,001, 7,348,444, and U.S. Pub. Pat. App. 2009/0234144.

All catalysts must first be started up in a manner to establish a good selectivity operation. U.S. Pat. No. 7,102,022 relates to the start-up of an epoxidation process wherein a highly selective catalyst is employed. In this patent there is disclosed an improved start-up procedure wherein the highly selective catalyst is subjected to a heat treatment wherein the catalyst is contacted with a feed comprising oxygen at a temperature above the normal operating temperature of the highly selective catalyst (i.e., above 260° C.). U.S. Pub. Pat. App. 2004/0049061 relates to a method of improving the selectivity of a highly selective catalyst having a low silver density. In this document, there is disclosed a method wherein the highly selective catalyst is subjected to a heat treatment which comprises contacting the catalyst with a feed comprising oxygen at a temperature above the normal operating temperature of the highly selective catalyst (i.e., above 250° C.). U.S. Pat. No. 4,874,879 relates to the start-up of an epoxidation process employing a highly selective catalyst wherein the highly selective catalyst is first contacted with a feed containing an organic chloride moderator and ethylene, and optionally a ballast gas, at a temperature below the normal operating temperature of the catalyst. EP-B1-1532125 relates to an improved start-up procedure wherein the highly selective catalyst is first subjected to a pre-soak phase in the presence of a feed containing an organic halide and is then subjected to a stripping phase in the presence of a feed which is free of the organic halide or may comprise the organic halide in a low quantity. The stripping phase is taught to continue for a period of more than 16 hours up to 200 hours. U.S. Pat. App. No. 2009/0281339 relates to the start-up where the organic chloride in the feed is adjusted to a value sufficient to produce EO at a substantially optimum selectivity.

At the end of the start-up period, the chloride level is typically adjusted to find the chloride level which gives the maximum selectivity at the desired EO production rate. The plant then sets the chloride level equal to this so-called “chloride optimum” and begins normal operation of the catalyst, which continues until it is discharged from the reactor. During normal operation of the catalyst, several routine things may happen:

-   -   The catalyst will deactivate. In order to maintain a constant         production rate, the reaction temperature will be increased as         the catalyst deactivates.     -   The production rate may change, due to feedstock availability,         production demands, or economics. To increase the production         rate, the reaction temperature will be increased; to decrease         the production rate, the reaction temperature will be decreased.     -   The feed composition may change. Generally, CO₂ levels will         increase over the life of the catalyst as selectivity drops.         Also, ethylene and oxygen levels may be changed due to feedstock         issues or to lower temperature near end-of-cycle.     -   Feed impurities (such as ethane or propane) may fluctuate.     -   There may be an upset in operation due to such events as         equipment failure or unplanned operation changes or deviations         from normal operation.

It is well-known (see, e.g., U.S. Pat. No. 7,193,094 and EP 1,458,698) that changes in reaction temperature or hydrocarbon concentration will change the chloride optimum. For example, as the reaction temperature increases or as hydrocarbon levels increase, the chloride level will also need to be increased in order to maintain operation at the maximum selectivity. During routine plant operation, the chloride level is adjusted in one of two methods:

-   -   1. The plant utilizes some proprietary mathematical formula         which relates chloride level to temperature, composition, etc.         This formula is computed periodically and if the chloride level         is found to be significantly different than the optimal level         (as determined by the formula), then the chloride level is         adjusted so that it equals the optimal level.     -   2. More frequently, the plant routinely checks whether the         chloride level is still optimized. This may happen at some fixed         frequency or following certain changes in operating conditions,         as determined by the plant. Typically, the chloride level is         increased or decreased slightly and the plant observes whether         the selectivity changed. If it did not change, then they were         probably operating at the selectivity maximum, so the chloride         level is reset to its original value. If the selectivity did         change, then the chloride level is changed in small steps until         a selectivity maximum is found, and then the plant continues         operation at this new chloride optimum.

Notwithstanding the improvements already achieved, there is a desire to further improve the performance of the silver-containing catalysts in the production of an olefin oxide, a 1,2-diol, a 1,2-diol ether, 1,2-carbonate or an alkanolamine.

SUMMARY OF THE INVENTION

The present invention shows that routine operation of a high-selectivity catalyst in the typical fashion described above is not truly optimal. It is believed that the processes that occur during start-up, namely exposure of the catalyst to high temperatures in the presence of low chloride levels, are necessary to distribute the catalyst dopants optimally. Incremental changes to the chloride level over the course of a catalyst run do not usually provide the proper conditions to maintain the optimal surface dopant configuration.

Significant increases in the selectivity of a catalyst may be obtained through conducting a “hard strip” according to the present invention, in which the feed chloride level is significantly reduced or eliminated for a period of time. After the hard strip, the chloride level is first returned to around the prior chloride level (i.e., the chloride level in use immediately prior to the hard strip). In one option the catalyst is re-optimized at that point in time. It was found that the claimed hard strip procedure may increase the catalyst selectivity by several selectivity points, with the greatest benefit being for catalysts that have lost significant selectivity over the course of the run due to aging. In such cases, selectivity gains as high as 3% were observed following a hard strip.

In accordance with this invention, the operation of an epoxidation process using a highly selective catalyst can be improved by utilizing the process steps according to the present invention. In particular, the present invention comprises a process for improving the selectivity of an ethylene epoxidation process employed in a reactor comprising a catalyst bed having a multitude of reactor tubes filled with a high selectivity epoxidation catalyst, said process comprising:

-   -   (a) contacting the catalyst bed with a feed comprising ethylene,         oxygen, and an organic chloride moderator for at least a period         of time T₁ to produce ethylene oxide;     -   (b) subsequently subjecting the high selectivity epoxidation         catalyst to a hard strip over a period of time T₂, which         comprises:         -   (i) significantly reducing the organic chloride added to the             feed; and         -   (ii) treating the catalyst in order to strip a portion of             the chlorides from the surface of the catalyst by increasing             the reactor temperature; and     -   (c) following the hard strip, increasing the quantity of organic         chloride added to the feed to a level of between 80 and 120% of         the prior concentration and reducing the reactor temperature to         within 5° C. of the prior reactor temperature level.

Step (a) of the present invention comprises the normal operation of the process to produce ethylene oxide according to the design parameters of the plant and process. According to the present invention, it is possible to improve operation and selectivity by inclusion of an intermediate stripping step (b), where the organic chloride feed is significantly reduced or stopped and the reactor temperature increased for a period of time until the chloride level on the catalyst surface is significantly reduced.

In an optional step following step (c) the various operating conditions may be re-optimized to achieve a new optimum selectivity prior to resuming normal operation. Normal operation would comprise subsequently contacting the catalyst bed with feed comprising ethylene, oxygen, and an organic chloride moderator.

The organic chloride for use in the present process is typically one or more chloro-hydrocarbons. Preferably, the organic chloride is selected from the group of methyl chloride, ethyl chloride, ethylene dichloride, vinyl chloride or a mixture thereof. The most preferred reaction modifiers are ethyl chloride, vinyl chloride and ethylene dichloride.

The selectivity (to ethylene oxide) indicates the molar amount of ethylene oxide in the reaction product compared with the total molar amount of ethylene converted. By high-selectivity is meant a catalyst with selectivity greater than 80 molar-%, preferably greater than 85.7 molar-%. One such catalyst is a rhenium containing catalyst, such as that disclosed in U.S. Pat. No. 4,766,105 or US 2009/0281345A1.

T₁ refers to the initial period of time following start-up and is defined as the time required to produce at least 0.1 kilotons (10⁵ kg) of ethylene oxide per cubic meter of catalyst. For the typical range of commercial workrates from 100 to 300 kg/m³/hour, this translates to about 14 to about 42 days. T₂ refers to the time period for the chloride strip and should be as short as possible in order to start producing EO at the same or better commercial rates as before the chloride strip. This T₂ time period is typically about 2 to 72 hours, more preferably about 4 to about 24 hours.

It appears that the long used process of initial optimization of the catalyst does not produce a catalyst that will remain optimum over the life of the catalyst. Rather, it appears that the distribution of chlorides on the catalyst cannot reach a true optimum until there is a stripping of the chlorides, followed by a reintroduction of the chlorides. This constitutes a previously unknown operational method of significantly improving EO production profitability. Stripping the catalyst is common practice during start-up, but subsequent stripping does not happen in normal operation. This is because during a chloride strip, selectivity and EO production both drop, leading to reduced production by the EO plant, and plant operators are unwilling to lose that production of EO. However, as shown in the present invention, the occasional “hard strip” of chlorides done according to the invention returns at least 0.5% or better selectivity improvement for an extended period of operation. Therefore, the implementation of occasional hard strips may constitute the preferred mode of operation of the EO catalyst in the future.

DETAILED DESCRIPTION OF THE INVENTION

Although the present epoxidation process may be carried out in many ways, it is preferred to carry it out as a gas phase process, i.e. a process in which the feed is contacted in the gas phase with the catalyst which is present as a solid material, typically in a packed bed. Generally the process is carried out as a continuous process. The reactor is typically equipped with heat exchange facilities to heat or cool the catalyst. As used herein, the feed is considered to be the composition which is contacted with the catalyst. As used herein, the catalyst temperature or the temperature of the catalyst bed is deemed to be the temperature approximately half-way through the catalyst bed.

When new catalysts as well as aged catalysts which, due to a plant shut-down, have been subjected to a prolonged shut-in period are utilized in the epoxidation process, it may be useful in some instances to pre-treat these catalysts prior to carrying out the start-up process by passing a sweeping gas over the catalyst at an elevated temperature. The sweeping gas is typically an inert gas, for example nitrogen or argon, or mixtures comprising nitrogen and/or argon. The elevated temperature converts a significant portion of organic nitrogen compounds which may have been used in the manufacture of the catalyst to nitrogen containing gases which are swept up in the gas stream and removed from the catalyst. In addition, any moisture may be removed from the catalyst. Typically, when the catalyst is loaded into the reactor, by utilizing the coolant heater, the temperature of the catalyst is brought up to 200 to 250° C., preferably from 210 to 230° C., and the gas flow is passed over the catalyst. Further details on this pre-treatment may be found in U.S. Pat. No. 4,874,879, which is incorporated herein by reference.

The catalyst is subjected to a start-up process which involves an initial step of contacting the catalyst with a feed comprising ethylene, oxygen, and an organic chloride. For the sake of clarity only, this step of the process will be indicated hereinafter by the term “initial start-up phase”. During the initial start-up phase, the catalyst is able to produce ethylene oxide at or near the selectivity experienced after the catalyst has “lined-out” under normal initial operating conditions after the start-up process. In particular, during the initial start-up phase, the selectivity may be within 3 mole-%, more in particular within 2 mole-%, most in particular within 1 mole-% of the optimum selectivity performance under normal initial operating conditions. Suitably, the selectivity may reach and be maintained at more than 86.5 mole-%, in particular at least 87 mole-%, more in particular at least 87.5 mole-% during the initial start-up phase. Since the selectivity of the catalyst quickly increases, there is advantageously additional production of ethylene oxide.

In the initial start-up phase, the catalyst is contacted with organic chloride for a period of time until an increase of at least 1×10⁻⁵ mole-% of vinyl chloride (calculated as the moles of vinyl chloride relative to the total gas mixture) is detected in the reactor outlet or the recycle gas loop. Without wishing to be bound by theory, when using organic chlorides other than vinyl chloride, it is believed that the vinyl chloride detected in the outlet or recycle loop is generated by the reaction of surface adsorbed chloride on the silver present in the catalyst with a C₂ hydrocarbon present in the feed. Preferably, the catalyst is contacted with organic chloride for a period of time until an increase of at least 2×10⁻⁵ mole-% of vinyl chloride, in particular at most 1×10⁻⁴ mole-% (calculated as the moles of vinyl chloride relative to the total gas mixture) is detected in the reactor outlet or the recycle gas loop. The quantity of organic chloride contacted with the catalyst during the initial start-up phase may be in the range of from 1 to 12 millimolar (mmolar) equivalent of chloride per kilogram of catalyst. The mmolar equivalent of chloride is determined by multiplying the mmoles of the organic chloride by the number of chloride atoms present in the organic chloride molecule, for example 1 mmole of ethylene dichloride provides 2 mmolar equivalent of chloride. The organic chloride may be fed to the catalyst bed for a period of time ranging from 1 to 15 hours, preferably 2 to 10 hours, more preferably from 2.5 to 8 hours. Suitably, the quantity of the organic chloride contacted with the catalyst may be at most 6 mmolar equivalent/kg catalyst, in particular at most 5.5 mmolar equivalent/kg catalyst, more in particular at most 5 mmolar equivalent/kg catalyst. The quantity of the organic chloride in the feed during the initial start-up phase may be at least 1.5×10⁻⁴ mole-%, in particular at least 2×10 mole-%, calculated as moles of chloride, relative to the total feed. The quantity of the organic chloride during the initial start-up phase may be at most 0.1 mole-%, preferably at most 0.01 mole-%, calculated as moles of chloride, relative to the total feed. Preferably, the initial start-up feed may comprise the organic chloride in a quantity above the optimum quantity used during the initial period of normal ethylene oxide production.

The feed during the initial start-up phase may also contain additional reaction modifiers which are not organic halides, such as nitrate- or nitrite-forming compounds, as described herein.

The feed during the initial start-up phase also contains ethylene. Ethylene may be present in the initial start-up feed in a quantity of at least 10 mole-%, preferably at least 15 mole-%, more preferably at least 20 mole-%, relative to the total feed. Ethylene may be present in the initial start-up feed in a quantity of at most 50 mole-%, preferably at most 45 mole-%, more preferably at most 40 mole-%, relative to the total feed. Preferably, ethylene may be present in the initial start-up feed in the same or substantially the same quantity as utilized during normal ethylene oxide production. This provides an additional advantage in that ethylene concentration does not have to be adjusted between the initial start-up phase and normal ethylene oxide production post start-up making the process more efficient.

The feed during the initial start-up phase also contains oxygen. The oxygen may be present in the initial start-up feed in a quantity of at least 1 mole-%, preferably at least 2 mole-%, more preferably at least 2.5 mole-%, relative to the total feed. The oxygen may be present in the initial start-up feed in a quantity of at most 15 mole-%, preferably at most 10 mole-%, more preferably at most 5 mole-%, relative to the total feed. It may be advantageous to apply a lower oxygen quantity in the initial start-up feed, compared with the feed composition in later stages of the process during normal ethylene oxide production since a lower oxygen quantity in the feed will reduce the oxygen conversion level so that, advantageously, hot spots in the catalyst are better avoided and the process will be more easily controllable.

The feed during the initial start-up phase may also contain carbon dioxide. The carbon dioxide may be present in the initial start-up feed in a quantity of at most 10 mole-%, preferably at most 5 mole-%, relative to the total feed. In an embodiment, the initial start-up phase also contains less than 2 mole-%, preferably less than 1.5 mole percent, more preferably less than 1.2 mole percent, most preferably less than 1 mole percent, in particular at most 0.75 mole percent carbon dioxide, relative to the total feed. In the normal practice of the present invention, the quantity of carbon dioxide present in the reactor feed is at least 0.1 mole percent, or at least 0.2 mole percent, or at least 0.3 mole percent, relative to the total feed. Suitably, the carbon dioxide may be present in the initial start-up feed in the same or substantially the same quantity as utilized during normal ethylene oxide production. The balance of the feed during the initial start-up phase may also contain an inert and/or saturated hydrocarbon.

During the initial start-up phase, the catalyst temperature preferably may be at substantially the same temperature as the normal initial catalyst operating temperature after the epoxidation process has “lined-out” under normal operating conditions after the start-up process. The term “substantially the same temperature” as used herein is meant to include catalyst temperatures within ±5° C. of the normal initial catalyst operating temperature after the epoxidation process has “lined-out” under normal operating conditions after the start-up process. Preferably, the catalyst temperature is less than 250° C., preferably at most 245° C. The catalyst temperature may be at least 200° C., preferably at least 220° C., more preferably at least 230° C. The reactor inlet pressure may be at most 4000 kPa absolute, preferably at most 3500 kPa absolute, more preferably at most 2500 kPa absolute. The reactor inlet pressure is at least 500 kPa absolute. The Gas Hourly Space Velocity or “GHSV”, defined hereinafter, may be in the range of from 500 to 10000 N1/(1. h).

During the initial start-up phase, the catalyst may first be contacted with a feed comprising ethylene and optionally a saturated hydrocarbon, in particular ethane and optionally methane. The organic chloride may then be added to the feed. The oxygen may be added to the feed simultaneously with or shortly after the first addition of the organic chloride to the feed. Within a few minutes of the addition of oxygen, the epoxidation reaction can initiate. Carbon dioxide and additional feed components may be added at any time, preferably simultaneously with or shortly after the first addition of oxygen to the initial start-up feed. As discussed above, during the initial start-up phase, the catalyst is able to produce ethylene oxide at or near the selectivity experienced after the catalyst has “lined-out” under normal initial operating conditions after the start-up process. During the initial start-up phase, the catalyst is operated under conditions such that ethylene oxide is produced at a level that is from 45 to 100% of the targeted production level during normal ethylene oxide production, in particular from 50 to 70%, same basis.

The present epoxidation process may be air-based or oxygen-based, see “Kirk-Othmer Encyclopedia of Chemical Technology”, 3^(rd) edition, Volume 9, 1980, pp. 445-447. In the air-based process, air or air enriched with oxygen is employed as the source of the oxidizing agent while in the oxygen-based processes, high-purity (at least 95 mole-%) or very high purity (at least 99.5 mole-%) oxygen is employed as the source of the oxidizing agent. Reference may be made to U.S. Pat. No. 6,040,467, incorporated by reference, for further description of oxygen-based processes. Presently most epoxidation plants are oxygen-based and this is a preferred embodiment of the present invention.

In addition to ethylene, oxygen and the organic chloride, the production feed during the normal epoxidation process may contain one or more optional components, such as nitrogen-containing reaction modifiers, carbon dioxide, inert gases and saturated hydrocarbons.

Nitrogen oxides, organic nitro compounds such as nitromethane, nitroethane, and nitropropane, hydrazine, hydroxylamine or ammonia may be employed as reaction modifiers in the epoxidation process. It is frequently considered that under the operating conditions of ethylene epoxidation the nitrogen containing reaction modifiers are precursors of nitrates or nitrites, i.e. they are so-called nitrate- or nitrite-forming compounds. Reference may be made to EP-A-3642 and U.S. Pat. No. 4,822,900, which are incorporated herein by reference, for further description of nitrogen-containing reaction modifiers.

Suitable nitrogen oxides are of the general formula NO_(x) wherein x is in the range of from 1 to 2.5, and include for example NO, N₂O₃, N₂O₄, and N₂O₅. Suitable organic nitrogen compounds are nitro compounds, nitroso compounds, amines, nitrates and nitrites, for example nitromethane, 1-nitropropane or 2-nitropropane.

Carbon dioxide is a by-product in the epoxidation process. However, carbon dioxide generally has an adverse effect on the catalyst activity, and high concentrations of carbon dioxide are therefore typically avoided. A typical epoxidation reactor feed during the normal epoxidation process may contain a quantity of carbon dioxide in the feed of at most 10 mole-%, relative to the total feed, preferably at most 5 mole-%, relative to the total feed. A quantity of carbon dioxide of less than 3 mole-%, preferably less than 2 mole-%, more preferably less than 1 mole-%, relative to the total feed, may be employed. Under commercial operations, a quantity of carbon dioxide of at least 0.1 mole-%, in particular at least 0.2 mole-%, relative to the total feed, may be present in the feed.

The inert gas may be, for example, nitrogen or argon, or a mixture thereof. Suitable saturated hydrocarbons are propane and cyclopropane, and in particular methane and ethane. Saturated hydrocarbons may be added to the feed in order to increase the oxygen flammability limit.

In the normal ethylene oxide production phase, the invention may be practiced by using methods known in the art of epoxidation processes. For further details of such epoxidation methods reference may be made, for example, to U.S. Pat. No. 4,761,394, U.S. Pat. No. 4,766,105, U.S. Pat. No. 6,372,925, U.S. Pat. No. 4,874,879, and U.S. Pat. No. 5,155,242, which are incorporated herein by reference.

In normal ethylene oxide production phase, the process may be carried out using reaction temperatures selected from a wide range. Preferably the reaction temperature is in the range of from 150 to 325° C., more preferably in the range of from 180 to 300° C.

In the normal ethylene oxide production phase, the concentration of the components in the feed may be selected within wide ranges, as described hereinafter.

The quantity of ethylene present in the production feed may be selected within a wide range. The quantity of ethylene present in the feed will be at most 80 mole-%, relative to the total feed. Preferably, it will be in the range of from 0.5 to 70 mole-%, in particular from 1 to 60 mole-%, on the same basis. Preferably, the quantity of ethylene in the production feed is substantially the same as used in the start-up process. If desired, the ethylene concentration may be increased during the lifetime of the catalyst, by which the selectivity may be improved in an operating phase wherein the catalyst has aged, see U.S. Pat. No. 6,372,925 which methods are incorporated herein by reference.

Often present in the feed will be saturated hydrocarbons such as ethane and methane. These saturated hydrocarbons are also termed “co-moderators”, since they have an impact on the effect of the chloride “moderators”, in that they are effective at removing or “stripping” adsorbed chloride from the surface of the catalyst. The level of ethane is typically 0.05 to 1.5 mole-% of the feed, more typically 0.05 to 0.5 mol-% of the feed, and will depend upon the particular feed stream to the reactor. Such level is monitored, but is not usually controlled during normal operation.

The quantity of oxygen present in the production feed may be selected within a wide range. However, in practice, oxygen is generally applied in a quantity which avoids the flammable regime. The quantity of oxygen applied will be within the range of from 4 to 15 mole-%, more typically from 5 to 12 mole-% of the total feed.

In order to remain outside the flammable regime, the quantity of oxygen present in the feed may be lowered as the quantity of ethylene is increased. The actual safe operating ranges depend, along with the feed composition, also on the reaction conditions such as the reaction temperature and the pressure.

The organic chlorides are generally effective as a reaction modifier when used in small quantities in the production feed, for example up to 0.1 mole-%, calculated as moles of chloride, relative to the total production feed, for example from 0.01×10⁴ to 0.01 mole-%, calculated as moles of chloride, relative to the total production feed. In particular, it is preferred that the organic chloride may be present in the feed in a quantity of from 1×10⁴ to 50×10⁴ mole-%, in particular from 1.5×10⁴ to 25×10⁴ mole-%, more in particular from 1.75×10⁴ to 20×10⁴ mole-%, calculated as moles of chloride, relative to the total production feed. When nitrogen containing reaction modifiers are applied, they may be present in low quantities in the feed, for example up to 0.1 mole-%, calculated as moles of nitrogen, relative to the total production feed, for example from 0.01×10⁴ to 0.01 mole-%, calculated as moles of nitrogen, relative to the total production feed. In particular, it is preferred that the nitrogen containing reaction modifier may be present in the feed in a quantity of from 0.05×10⁴ to 50×10⁴ mole-%, in particular from 0.2×10⁴ to 30×10⁴ mole-%, more in particular from 0.5×10⁴ to 10×10⁴ mole-%, calculated as moles of nitrogen, relative to the total production feed.

Inert gases, for example nitrogen or argon, may be present in the production feed in a quantity of 0.5 to 90 mole-%, relative to the total feed. In an air based process, inert gas may be present in the production feed in a quantity of from 30 to 90 mole-%, typically from 40 to 80 mole-%. In an oxygen-based process, inert gas may be present in the production feed in a quantity of from 0.5 to 30 mole-%, typically from 1 to 15 mole-%. If saturated hydrocarbons are present, they may be present in a quantity of up to 80 mole-%, relative to the total production feed, in particular up to 75 mole-%, same basis. Frequently they are present in a quantity of at least 30 mole-%, more frequently at least 40 mole-%, same basis.

In the normal ethylene oxide production phase, the epoxidation process is preferably carried out at a reactor inlet pressure in the range of from 1000 to 3500 kPa. “GHSV” or Gas Hourly Space Velocity is the unit volume of gas at normal temperature and pressure (0° C., 1 atm, i.e. 101.3 kPa) passing over one unit volume of packed catalyst per hour. Preferably, when the epoxidation process is a gas phase process involving a packed catalyst bed, the GHSV is in the range of from 1500 to 10000 N1/(1. h). Preferably, the process is carried out at a work rate in the range of from 0.5 to 10 kmole ethylene oxide produced per m³ of catalyst per hour, in particular 0.7 to 8 kmole ethylene oxide produced per m³ of catalyst per hour, for example 5 kmole ethylene oxide produced per m³ of catalyst per hour. As used herein, the work rate is the amount of ethylene oxide produced per unit volume of catalyst per hour and the selectivity is the molar quantity of ethylene oxide formed relative to the molar quantity of ethylene converted.

The key to the present invention is to initiate a “hard strip” of the chlorides following the initial start-up of the process and after a partial production of the planned EO run, but prior to the planned shut down and catalyst replacement. In the past, EO plant operators would not consider a “hard strip”, but would rather alter operations by increasing reactor temperature and/or changing the relative amount of the chloride moderator in order to improve activity and/or selectivity as the catalyst degraded over time. This would continue until it became necessary to shut down the plant in order to remove the old degraded catalyst and replace it with a new catalyst. Now it has been discovered that there is an economic incentive to introduce a hard strip of the chlorides during the normal operation. Stripping of the chlorides is accomplished by first stopping or significantly reducing the introduction of fresh chloride moderator and increasing reactor temperature. The normal level of chloride addition is a function of catalyst, temperature, gas flowrate and catalyst volume. Significantly reducing the amount means to reduce the introduction of fresh chloride moderator into the feed stream to the reactor by at least 50%, more preferably at least 75% and most preferably by eliminating all the fresh addition of chloride (100% reduction). In order to strip a portion of the chlorides from the surface of the catalyst it will typically also be necessary to increase the reactor temperature by about 1 to about 30° C., preferably by about 2 to about 15° C.

Following the chloride strip, the chloride is then reintroduced over a relatively short time period until the level reaches approximately the same as prior to the hard strip. As for the time period for the hard strip, this should be as short as possible to effect the desired result in order to start producing EO at the same or better commercial rates as before the hard strip. This time period is typically about 2 to 72 hours, more preferably about 4 to about 24 hours.

Following the hard strip, the process may be continued under normal plant conditions. In an optional step the process may be re-optimized following the hard strip. This may be done by varying the chloride moderator up and down to determine at what level the selectivity is at substantially an optimum. This optimization step is fully described in U.S. Pat. No. 7,193,094 and US Published Application No. 2009/0281339, which disclosures are hereby incorporated by reference.

Following the first “hard strip”, the hard strip may be repeated later in the run as needed (e.g., if selectivity drops below expectations).

The epoxidation catalyst is a supported catalyst. The carrier may be selected from a wide range of materials. Such carrier materials may be natural or artificial inorganic materials and they include silicon carbide, clays, pumice, zeolites, charcoal, and alkaline earth metal carbonates, such as calcium carbonate. Preferred are refractory carrier materials, such as alumina, magnesia, zirconia, silica, and mixtures thereof. The most preferred carrier material is a-alumina.

The surface area of the carrier may suitably be at least 0.1 m²/g, preferably at least 0.3 m²/g, more preferably at least 0.5 m²/g, and in particular at least 0.6 m²/g, relative to the weight of the carrier; and the surface area may suitably be at most 20 m²/g, preferably at most 10 m²/g, more preferably at most 6 m²/g, and in particular at most 4 m²/g, relative to the weight of the carrier. “Surface area” as used herein is understood to relate to the surface area as determined by the B.E.T. (Brunauer, Emmett and Teller) method as described in Journal of the American Chemical Society 60 (1938) pp. 309-316. High surface area carriers, in particular when they are alpha alumina carriers optionally comprising in addition silica, alkali metal and/or alkaline earth metal components, provide improved performance and stability of operation.

The water absorption of the carrier may suitably be at least 0.2 g/g, preferably at least 0.25 g/g, more preferably at least 0.3 g/g, most preferably at least 0.35 g/g; and the water absorption may suitably be at most 0.85 g/g, preferably at most 0.7 g/g, more preferably at most 0.65 g/g, most preferably at most 0.6 g/g. The water absorption of the carrier may be in the range of from 0.2 to 0.85 g/g, preferably in the range of from 0.25 to 0.7 g/g, more preferably from 0.3 to 0.65 g/g, most preferably from 0.42 to 0.52 g/g. A higher water absorption may be in favor in view of a more efficient deposition of the metal and promoters on the carrier by impregnation. However, at a higher water absorption, the carrier, or the catalyst made therefrom, may have lower crush strength. As used herein, water absorption is deemed to have been measured in accordance with ASTM C20, and water absorption is expressed as the weight of the water that can be absorbed into the pores of the carrier, relative to the weight of the carrier.

A carrier may be washed, to remove soluble residues, before deposition of the catalyst ingredients on the carrier. Additionally, the materials used to form the carrier, including the burnout materials, may be washed to remove soluble residues. Such carriers are described in U.S. Pat. No. 6,368,998 and W0-A2-2007/095453, which are incorporated herein by reference. On the other hand, unwashed carriers may also be used successfully. Washing of the carrier generally occurs under conditions effective to remove most of the soluble and/or ionizable materials from the carrier.

The washing liquid may be, for example water, aqueous solutions comprising one or more salts, or aqueous organic diluents. Suitable salts for inclusion in an aqueous solution may include, for example ammonium salts. Suitable ammonium salts may include, for example ammonium nitrate, ammonium oxalate, ammonium fluoride, and ammonium carboxylates, such as ammonium acetate, ammonium citrate, ammonium hydrogencitrate, ammonium formate, ammonium lactate, and ammonium tartrate. Suitable salts may also include other types of nitrates such as alkali metal nitrates, for example lithium nitrate, potassium nitrate and cesium nitrate. Suitable quantities of total salt present in the aqueous solution may be at least 0.001% w, in particular at least 0.005% w, more in particular at least 0.01% w and at most 10% w, in particular at most 1% w, for example 0.03% w. Suitable organic diluents which may or may not be included are, for example, one or more of methanol, ethanol, propanol, isopropanol, tetrahydrofuran, ethylene glycol, ethylene glycol dimethyl ether, diethylene glycol dimethyl ether, dimethylformamide, acetone, or methyl ethyl ketone.

The preparation of the silver catalyst is known in the art and the known methods are applicable to the preparation of the catalyst which may be used in the practice of the present invention. Methods of depositing silver on the carrier include impregnating the carrier or carrier bodies with a silver compound containing cationic silver and/or complexed silver and performing a reduction to form metallic silver particles. For further description of such methods, reference may be made to U.S. Pat. No. 5,380,697, U.S. Pat. No. 5,739,075, U.S. Pat. No. 4,766,105, and U.S. Pat. No. 6,368,998, which are incorporated herein by reference. Suitably, silver dispersions, for example silver sols, may be used to deposit silver on the carrier.

The reduction of cationic silver to metallic silver may be accomplished during a step in which the catalyst is dried, so that the reduction as such does not require a separate process step. This may be the case if the silver containing impregnation solution comprises a reducing agent, for example, an oxalate, a lactate or formaldehyde.

Appreciable catalytic activity is obtained by employing a silver content of the catalyst of at least 10 g/kg, relative to the weight of the catalyst. Preferably, the catalyst comprises silver in a quantity of from 10 to 500 g/kg, more preferably from 50 to 450 g/kg, for example 105 g/kg, or 120 g/kg, or 190 g/kg, or 250 g/kg, or 350 g/kg. As used herein, unless otherwise specified, the weight of the catalyst is deemed to be the total weight of the catalyst including the weight of the carrier and catalytic components.

In an embodiment, the catalyst employs a silver content of the catalyst of at least 150 g/kg, relative to the weight of the catalyst. Preferably, the catalyst comprises silver in a quantity of from 150 to 500 g/kg, more preferably from 170 to 450 g/kg, for example 190 g/kg, or 250 g/kg, or 350 g/kg.

The catalyst for use in the present invention additionally comprises a rhenium promoter component. The form in which the rhenium promoter may be deposited onto the carrier is not material to the invention. For example, the rhenium promoter may suitably be provided as an oxide or as an oxyanion, for example, as a rhenate or perrhenate, in salt or acid form.

The rhenium promoter may be present in a quantity of at least 0.01 mmole/kg, preferably at least 0.1 mmole/kg, more preferably at least 0.5 mmole/kg, most preferably at least 1 mmole/kg, in particular at least 1.25 mmole/kg, more in particular at least 1.5 mmole/kg, calculated as the total quantity of the element relative to the weight of the catalyst. The rhenium promoter may be present in a quantity of at most 500 mmole/kg, preferably at most 50 mmole/kg, more preferably at most 10 mmole/kg, calculated as the total quantity of the element relative to the weight of the catalyst.

In an embodiment, the rhenium promoter is present in a quantity of at least 1.75 mmole/kg, preferably at least 2 mmole/kg, calculated as the total quantity of the element relative to the weight of the catalyst. The rhenium promoter may be present in a quantity of at most 15 mmole/kg, preferably at most 10 mmole/kg, more preferably at most 8 mmole/kg, calculated as the total quantity of the element relative to the weight of the catalyst.

In an embodiment, the catalyst may further comprise a potassium promoter deposited on the carrier. The potassium promoter may be deposited in a quantity of at least 0.5 mmole/kg, preferably at least 1 mmole/kg, more preferably at least 1.5 mmole/kg, most preferably at least 1.75 mmole/kg, calculated as the total quantity of the potassium element deposited relative to the weight of the catalyst. The potassium promoter may be deposited in a quantity of at most 20 mmole/kg, preferably at most 15 mmole/kg, more preferably at most 10 mmole/kg, most preferably at most 5 mmole/kg, on the same basis. The potassium promoter may be deposited in a quantity in the range of from 0.5 to 20 mmole/kg, preferably from 1 to 15 mmole/kg, more preferably from 1.5 to 7.5 mmole/kg, most preferably from 1.75 to 5 mmole/kg, on the same basis. A catalyst prepared in accordance with the present invention can exhibit an improvement in selectivity, activity, and/or stability of the catalyst especially when operated under conditions where the reaction feed contains low levels of carbon dioxide.

The catalyst for use in the present invention may additionally comprise a rhenium co-promoter. The rhenium co-promoter may be selected from tungsten, molybdenum, chromium, sulfur, phosphorus, boron, and mixtures thereof.

The rhenium co-promoter may be present in a total quantity of at least 0.1 mmole/kg, more typically at least 0.25 mmole/kg, and preferably at least 0.5 mmole/kg, calculated as the element (i.e. the total of tungsten, chromium, molybdenum, sulfur, phosphorus and/or boron), relative to the weight of the catalyst. The rhenium co-promoter may be present in a total quantity of at most 40 mmole/kg, preferably at most 10 mmole/kg, more preferably at most 5 mmole/kg, on the same basis. The form in which the rhenium co-promoter may be deposited on the carrier is not material to the invention. For example, it may suitably be provided as an oxide or as an oxyanion, for example, as a sulfate, borate or molybdate, in salt or acid form.

In an embodiment, the catalyst contains the rhenium promoter and tungsten in a molar ratio of the rhenium promoter to tungsten of greater than 2, more preferably at least 2.5, most preferably at least 3. The molar ratio of the rhenium promoter to tungsten may be at most 20, preferably at most 15, more preferably at most 10.

In an embodiment, the catalyst comprises the rhenium promoter and additionally a first co-promoter component and a second co-promoter component. The first co-promoter may be selected from sulfur, phosphorus, boron, and mixtures thereof. It is particularly preferred that the first co-promoter comprises, as an element, sulfur. The second co-promoter component may be selected from tungsten, molybdenum, chromium, and mixtures thereof. It is particularly preferred that the second co-promoter component comprises, as an element, tungsten and/or molybdenum, in particular tungsten. The form in which the first co-promoter and second co-promoter components may be deposited onto the carrier is not material to the invention. For example, the first co-promoter and second co-promoter components may suitably be provided as an oxide or as an oxyanion, for example, as a tungstate, molybdate, or sulfate, in salt or acid form.

In this embodiment, the first co-promoter may be present in a total quantity of at least 0.2 mmole/kg, preferably at least 0.3 mmole/kg, more preferably at least 0.5 mmole/kg, most preferably at least 1 mmole/kg, in particular at least 1.5 mmole/kg, more in particular at least 2 mmole/kg, calculated as the total quantity of the element (i.e., the total of sulfur, phosphorus, and/or boron) relative to the weight of the catalyst. The first co-promoter may be present in a total quantity of at most 50 mmole/kg, preferably at most 40 mmole/kg, more preferably at most 30 mmole/kg, most preferably at most 20 mmole/kg, in particular at most 10 mmole/kg, more in particular at most 6 mmole/kg, calculated as the total quantity of the element relative to the weight of the catalyst.

In this embodiment, the second co-promoter component may be present in a total quantity of at least 0.1 mmole/kg, preferably at least 0.15 mmole/kg, more preferably at least 0.2 mmole/kg, most preferably at least 0.25 mmole/kg, in particular at least 0.3 mmole/kg, more in particular at least 0.4 mmole/kg, calculated as the total quantity of the element (i.e., the total of tungsten, molybdenum, and/or chromium) relative to the weight of the catalyst. The second co-promoter may be present in a total quantity of at most 40 mmole/kg, preferably at most 20 mmole/kg, more preferably at most 10 mmole/kg, most preferably at most 5 mmole/kg, calculated as the total quantity of the element relative to the weight of the catalyst.

In an embodiment, the molar ratio of the first co-promoter to the second co-promoter may be greater than 1. In this embodiment, the molar ratio of the first co-promoter to the second co-promoter may preferably be at least 1.25, more preferably at least 1.5, most preferably at least 2, in particular at least 2.5. The molar ratio of the first co-promoter to the second co-promoter may be at most 20, preferably at most 15, more preferably at most 10.

In an embodiment, the molar ratio of the rhenium promoter to the second co-promoter may be greater than 1. In this embodiment, the molar ratio of the rhenium promoter to the second co-promoter may preferably be at least 1.25, more preferably at least 1.5. The molar ratio of the rhenium promoter to the second co-promoter may be at most 20, preferably at most 15, more preferably at most 10.

In an embodiment, the catalyst comprises the rhenium promoter in a quantity of greater than 1 mmole/kg, relative to the weight of the catalyst, and the total quantity of the first co-promoter and the second co-promoter deposited on the carrier may be at most 12 mmole/kg, calculated as the total quantity of the elements (i.e., the total of sulfur, phosphorous, boron, tungsten, molybdenum and/or chromium) relative to the weight of the catalyst. In this embodiment, the total quantity of the first co-promoter and the second co-promoter may preferably be at most 10 mmole/kg, more preferably at most 8 mmole/kg of catalyst. In this embodiment, the total quantity of the first co-promoter and the second co-promoter may preferably be at least 0.1 mmole/kg, more preferably at least 0.5 mmole/kg, most preferably at least 1 mmole/kg of the catalyst.

The catalyst may preferably further comprise a further element deposited on the carrier. Eligible further elements may be one or more of nitrogen, fluorine, alkali metals, alkaline earth metals, titanium, hafnium, zirconium, vanadium, thallium, thorium, tantalum, niobium, gallium and germanium and mixtures thereof. Preferably, the alkali metals are selected from lithium, sodium and/or cesium. Preferably, the alkaline earth metals are selected from calcium, magnesium and barium. Preferably, the further element may be present in the catalyst in a total quantity of from 0.01 to 500 mmole/kg, more preferably from 0.5 to 100 mmole/kg, calculated as the total quantity of the element relative to the weight of the catalyst. The further element may be provided in any form. For example, salts or hydroxides of an alkali metal or an alkaline earth metal are suitable. For example, lithium compounds may be lithium hydroxide or lithium nitrate.

In an embodiment, the catalyst may comprise cesium as a further element in a quantity of more than 1.0 mmole/kg, in particular at least 2.0 mmole/kg, more in particular at least 3.0 mmole/kg, calculated as the total quantity of the element relative to the weight of the catalyst. In this embodiment, the catalyst may comprise cesium in a quantity of at most 20 mmole/kg, in particular at most 15 mmole/kg, calculated as the total quantity of the element relative to the weight of the catalyst As used herein, unless otherwise specified, the quantity of alkali metal present in the catalyst and the quantity of water leachable components present in the carrier are deemed to be the quantity insofar as it can be extracted from the catalyst or carrier with de-ionized water at 100° C. The extraction method involves extracting a 10-gram sample of the catalyst or carrier three times by heating it in 20 ml portions of de-ionized water for 5 minutes at 100° C. and determining in the combined extracts the relevant metals by using a known method, for example atomic absorption spectroscopy.

As used herein, unless otherwise specified, the quantity of alkaline earth metal present in the catalyst and the quantity of acid leachable components present in the carrier are deemed to be the quantity insofar as it can be extracted from the catalyst or carrier with 10% w nitric acid in de-ionized water at 100° C. The extraction method involves extracting a 10-gram sample of the catalyst or carrier by boiling it with a 100 ml portion of 10% w nitric acid for 30 minutes (1 atm., i.e. 101.3 kPa) and determining in the combined extracts the relevant metals by using a known method, for example atomic absorption spectroscopy. Reference is made to U.S. Pat. No. 5,801,259, which is incorporated herein by reference.

Ethylene oxide produced may be recovered from the product mix by using methods known in the art, for example by absorbing ethylene oxide from a reactor outlet stream in water and optionally recovering ethylene oxide from the aqueous solution by distillation. At least a portion of the aqueous solution containing ethylene oxide may be applied in a subsequent process for converting ethylene oxide into a 1,2-diol, a 1,2-diol ether, a 1,2-carbonate, or an alkanolamine, in particular ethylene glycol, ethylene glycol ethers, ethylene carbonate, or alkanol amines.

Ethylene oxide produced in the epoxidation process may be converted into a 1,2-diol, a 1,2-diol ether, a 1,2-carbonate, or an alkanolamine. As this invention leads to a more attractive process for the production of ethylene oxide, it concurrently leads to a more attractive process which comprises producing ethylene oxide in accordance with the invention and the subsequent use of the obtained ethylene oxide in the manufacture of the 1,2-diol, 1,2-diol ether, 1,2-carbonate, and/or alkanolamine.

The conversion into the 1,2-diol (i.e., ethylene glycol) or the 1,2-diol ether (i.e., ethylene glycol ethers) may comprise, for example, reacting ethylene oxide with water, suitably using an acidic or a basic catalyst. For example, for making predominantly the 1,2-diol and less 1,2-diol ether, ethylene oxide may be reacted with a ten fold molar excess of water, in a liquid phase reaction in presence of an acid catalyst, e.g. 0.5-1.0% w sulfuric acid, based on the total reaction mixture, at 50-70° C. at 1 bar absolute, or in a gas phase reaction at 130-240° C. and 20-40 bar absolute, preferably in the absence of a catalyst. The presence of such a large quantity of water may favor the selective formation of 1,2-diol and may function as a sink for the reaction exotherm, helping control the reaction temperature. If the proportion of water is lowered, the proportion of 1,2-diol ethers in the reaction mixture is increased. Alternative 1,2-diol ethers may be prepared by converting ethylene oxide with an alcohol, in particular a primary alcohol, such as methanol or ethanol, by replacing at least a portion of the water by the alcohol.

Ethylene oxide may be converted into the corresponding 1,2-carbonate by reacting ethylene oxide with carbon dioxide. If desired, ethylene glycol may be prepared by subsequently reacting the 1,2-carbonate with water or an alcohol to form the glycol. For applicable methods, reference is made to U.S. Pat. No. 6,080,897, which is incorporated herein by reference.

The conversion into the alkanolamine may comprise, for example, reacting ethylene oxide with ammonia. Anhydrous ammonia is typically used to favor the production of monoalkanolamine. For methods applicable in the conversion of ethylene oxide into the alkanolamine, reference may be made to, for example U.S. Pat. No. 4,845,296, which is incorporated herein by reference.

The 1,2-diol and the 1,2-diol ether may be used in a large variety of industrial applications, for example in the fields of food, beverages, tobacco, cosmetics, thermoplastic polymers, curable resin systems, detergents, heat transfer systems, etc. The 1,2-carbonates may be used as a diluent, in particular as a solvent. The alkanolamine may be used, for example, in the treating (“sweetening”) of natural gas.

Example 1

A “tube fraction” is a sample of catalyst that has been removed from a commercial EO reactor after an extended period of commercial operation, with each fraction representing a specific axial region of a specific reactor tube. In Example 1, an assortment of tube fractions were subjected to microreactor testing at the conclusion of a commercial high selectivity catalyst cycle at Plant A. The following parameters were used in our tests in order to closely simulate the average commercial operation conditions for Plant A: Feedstock: 27.5% v C₂H₄, 7.3% v O₂, 1.4% v CO₂; variable amounts of ethyl chloride moderator, balance N₂. Conditions: 4680 hr⁻¹ Gas Hourly Space Velocity, 19.5 barg pressure, 253 kg/m³/hr workrate.

To demonstrate the instant invention in our microreactors, a two-step testing protocol was utilized. It is important to appreciate that Step 1 is not the inventive step per se, but rather, provides critical information that is required prior to performing the inventive step. The objective of Step 1 was to identify the “chloride optimum” for a given catalyst as it operates at the above-specified conditions in our microreactor, which is to say, to identify the concentration of ethyl chloride “EC-opt” for which the maximum selectivity is achieved at the specified conditions. A properly operated commercial plant should already know the optimum level of chloride for their catalyst at their current conditions. However, the chloride optimum reported by the plant frequently does not exactly correspond to the chloride optimum that we observe in our microreactor testing. For this reason, unlike a commercial plant wishing to employ the instant invention, Step 1 must be employed to identify the chloride optimum of each sample in our microreactors prior to performing the instant invention. To employ the instant invention, a commercial plant needs only apply the procedure described below as Step 2.

To properly identify the chloride optimum, one must take care to begin the optimization procedure at a chloride level that is below the optimum level and continue stepwise increasing the chloride level until above the optimum level, collecting equilibrated performance data at each chloride level, and thereby tracing out a selectivity-versus-chloride curve that displays a region of maximum selectivity lying somewhere between the terminal points of the curve.

A catalyst is said to be “undermoderated” when the amount of chloride on the catalyst surface and the amount of chloride in the gas phase are in equilibrium, and said chloride level on the catalyst surface is less than the amount required to achieve maximum selectivity. To render the catalyst into an undermoderated state, one can select from many combinations of catalyst temperature and chloride level in the gas phase. For example, one can hold the catalyst temperature constant at its “normal” operating level, and reduce or entirely eliminate the chloride content of the gas stream for a period of time. In that scenario, lower levels of chloride are preferable, since the time required to drive the catalyst into an undermoderated state is related to the degree of undermoderation. As a second example, one can hold the chloride concentration of the feed stream at its “normal” operating level, and elevate the temperature of the catalyst. As a third example, one can manipulate both the temperature and the chloride level in order to induce an undermoderated state.

In each test comprising Example 1, operation commenced at a constant catalyst temperature of 240° C. while including 1.2 ppmv moderator in the feed stream for 8 hours. Moderator flow was reduced to zero while catalyst temperature was held at 240° C. for a period of 4 hours, and then sequentially increased to 247° C. for a period of 4 hours, and to 255° C. for a period of 8 hours. Moderator flow was then re-introduced at a level of 1.5 ppmv for a period of 36 hours, at which time the reactor was placed on workrate control at the target workrate. The moderator level was then sequentially incremented every 36 hours to 1.8, 2.1, 2.4, 2.7 and 3.0 ppmv in order to identify the optimal concentration of chloride “EC-opt”, the corresponding or “optimized” selectivity, and the corresponding catalyst temperature. In the Table, optimized catalyst performance data are shown in the columns labeled “Performance Prior to Temperature Treatment”.

Step 2 of the testing protocol was to perform the steps comprising the instant invention. The catalyst was again subjected to a chloride strip at 240° C. for a period of 4 hours, 247° C. for a period of 4 hours, and then 255° C. for a period of 8 hours. Following the chloride strip, moderator flow was re-introduced. However, unlike the protocol for moderator introduction protocol described earlier, this time the moderator flow was re-introduced precisely at the level that had previously been identified as “optimal”. After selectivity and temperature reached equilibrium, performance data were again recorded—see columns labeled “Performance Following Temperature Treatment”. The improvement that we observed following Step 2 is shown in the column “Improvement in Selectivity”.

EXAMPLE 1 - Commercially Aged High Selectivity Catalyst. Performance Performance Prior To Following Micro- Temperature Temperature reactor Treatment Treatment Improve- Bed No. Selec- Catalyst Selec- Catalyst ment In Catalyst LR-27126 tivity Temp tivity Temp Selectivity Sample LR*27139 (%) (° C.) (%) (° C.) (%) 1 -104-2 81.9 259 84.1 256 2.2 2 -104-3 81.1 259 83.2 259 2.1 3 -104-1 81.7 243 84.1 246 2.4 4 -104-4 81.7 248 83.1 251 1.4 5 -133-2 81.5 255 82.4 256 0.9 6 *003-2 81.1 257 83.2 254 2.1 7 *003-3 81.2 253 83.6 251 2.4 8 *003-1 79.8 244 82.2 245 2.4 9 *003-4 80.6 247 83.1 247 2.5 10 *007-1 81.2 250 83.8 249 2.6 11 *007-2 80.4 250 82.3 249 1.9 12 *007-3 81.6 250 82.3 248 0.7 Average all sections: 81.2 251 83.1 251 2.0

Example 2

In Example 2, the same protocol as outlined above was followed for a different set of commercially aged high selectivity catalyst samples from Plant B. Results are summarized in the Table “Example 2—Commercially Aged High Selectivity Catalyst”.

EXAMPLE 2 - Commercially Aged High Selectivity Catalyst. Performance Performance Prior To Following Micro- Temperature Temperature reactor Treatment Treatment Improve- Bed No. Selec- Catalyst Selec- Catalyst ment In Catalyst LR-27126 tivity Temp tivity Temp Selectivity Sample LR*27139 (%) (° C.) (%) (° C.) (%) 1 -014-2 79.7 244 82.5 242 2.8 2 *138-4 79.5 242 82.0 241 2.5 3 -036-3 80.5 243 83.4 240 2.9 4 -026-1 81.1 242 83.6 242 2.5 5 -026-4 81.8 242 84.0 240 2.2 Average all sections: 80.5 242 83.1 241 2.6

Example 3

In Example 3 an experiment was run to show the effect of increasing the temperature to affect a hard strip. In this experiment 4.6 grams of a rhenium containing high selectivity catalyst according to US 2009/0281345A1 was loaded into a U-tube reactor at 14-20 mesh size. The catalyst was operated for 10 months at 30 mole-% ethylene, 8 mole-% oxygen, 1 mole-% carbon dioxide with the balance nitrogen and a reactor inlet pressure of 210 psig, with an EO concentration of 3.09%. The ethyl chloride (EC) moderator was adjusted periodically to maintain maximum selectivity. After 10 months of operation the selectivity declined to 88%, the EC concentration was 4.2 ppm and the catalyst temperature was 249.2° C. A hard strip was performed according to the claimed invention by increasing the temperature to 250.2° C. and decreasing the EC concentration to ZERO for 6 hours and then resetting the EC concentration to 3.9 ppm. The catalyst temperature was adjusted to make 3.09% EO. The resulting catalyst selectivity was 89.4% at 249.2° C., an INCREASE of 1.4% with no change in temperature. 

1. A process for improving the selectivity of an ethylene epoxidation process employed in a reactor comprising a catalyst bed having a multitude of reactor tubes filled with a high selectivity epoxidation catalyst, said process comprising: (a) contacting the catalyst bed with a feed comprising ethylene, oxygen, and an organic chloride moderator for at least a period of time T₁ to produce ethylene oxide; (b) subsequently subjecting the high selectivity epoxidation catalyst to a hard strip over a period of time T₂, which comprises: (i) significantly reducing the organic chloride moderator added to the feed; and (ii) treating the catalyst in order to strip a portion of the chlorides from the surface of the catalyst by increasing the reactor temperature; and (c) following the hard strip increasing the quantity of organic chloride added to the feed to a level of between 80 and 120% of the prior concentration and reducing the reactor temperature to within 5° C. of the prior reactor temperature level.
 2. The process of claim 1 wherein said organic chloride moderator is selected from the group consisting of methyl chloride, ethyl chloride, ethylene dichloride, vinyl chloride and mixtures thereof.
 3. The process of claim 2 wherein the quantity of fresh organic chloride added with the feed in step (a) is in the range of from 0.01×10⁻⁴ to 2×10⁻³ mole-%, calculated as moles of chloride, relative to the total feed.
 4. The process of claim 3 wherein the quantity of the fresh organic chloride added in the feed is reduced by 50 to 100 percent during step (b) hard strip.
 5. The process of claim 4 wherein the reactor temperature is increased by about 1 to about 30° C. during the step (b) hard strip.
 6. The process of claim 4 wherein the reactor temperature is increased by about 2 to about 15° C. during the step (b) hard strip.
 7. The process of claim 4 wherein T₁ is the period of time after startup and after production of about 0.1 kilotons ethylene oxide per cubic meter of catalyst and T₂ is about 2 hours to about 72 hours.
 8. The process of claim 7 wherein T₂ is about 4 to 24 hours.
 9. The process of claim 4 wherein said high selectivity epoxidation catalyst comprises a carrier and, deposited on the carrier, silver, a rhenium promoter, a first co-promoter, and a second co-promoter; wherein: a) the quantity of the rhenium promoter deposited on the carrier is greater than 1 mmole/kg, relative to the weight of the catalyst; b) the first co-promoter is selected from sulfur, phosphorus, boron, and mixtures thereof; and c) the second co-promoter is selected from tungsten, molybdenum, chromium, and mixtures thereof.
 10. The process of claim 9 wherein the total quantity of the first co-promoter and the second co-promoter deposited on the carrier is at most 10.0 mmole/kg, relative to the weight of the catalyst; and said carrier has a monomodal, bimodal or multimodal pore size distribution, with a pore diameter range of 0.01-200 μm, a specific surface area of 0.03-10 m²/g, a pore volume of 0.2-0.7 cm³/g, wherein the median pore diameter of said carrier is 0.1-100 μm and has a water absorption of 10-80%.
 11. The process of claim 10 wherein the CO₂ in the feed is less than 2%.
 12. A process for preparing a 1,2-diol, a 1,2-diol ether, a 1,2-carbonate, or an alkanolamine comprising converting ethylene oxide into the 1,2-diol, the 1,2-diol ether, the 1,2-carbonate, or the alkanolamine wherein the ethylene oxide has been prepared by the process as claimed in claim
 1. 